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Estela Maria Bruxel

TitlePostdoc Fellows and Associates
InstitutionBaylor College of Medicine
DepartmentPostDoc
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Bruxel EM, Rovaris DL, Belangero SI, Chavarr?a-Soley G, Cuellar-Barboza AB, Mart?nez-Maga?a JJ, Nagamatsu ST, Nievergelt CM, N??ez-R?os DL, Ota VK, Peterson RE, Sloofman LG, Adams AM, Albino E, Alvarado AT, Andrade-Brito D, Arguello-Pascualli PY, Bandeira CE, Bau CHD, Bulik CM, Buxbaum JD, Cappi C, Corral-Frias NS, Corrales A, Corsi-Zuelli F, Crowley JJ, Cupertino RB, da Silva BS, De Almeida SS, De la Hoz JF, Forero DA, Fries GR, Gelernter J, Gonz?lez-Giraldo Y, Grevet EH, Grice DE, Hern?ndez-Garayua A, Hettema JM, Ib??ez A, Ionita-Laza I, Lattig MC, Lima YC, Lin YS, L?pez-Le?n S, Loureiro CM, Mart?nez-Cerde?o V, Mart?nez-Levy GA, Melin K, Moreno-De-Luca D, Muniz Carvalho C, Olivares AM, Oliveira VF, Ormond R, Palmer AA, Panzenhagen AC, Passos-Bueno MR, Peng Q, P?rez-Palma E, Prieto ML, Roussos P, Sanchez-Roige S, Santamar?a-Garc?a H, Shansis FM, Sharp RR, Storch EA, Tavares MEA, Tietz GE, Torres-Hern?ndez BA, Tovo-Rodrigues L, Trelles P, Trujillo-ChiVacuan EM, Vel?squez MM, Vera-Urbina F, Voloudakis G, Wegman-Ostrosky T, Zhen-Duan J, Zhou H, Latin American Genomics Consortium, Santoro ML, Nicolini H, Atkinson EG, Giusti-Rodr?guez P, Montalvo-Ortiz JL. Psychiatric genetics in the diverse landscape of Latin American populations. Nat Genet. 2025 May; 57(5):1074-1088. PMID: 40175716; PMCID: PMC12133068.
      Citations:    Fields:    
    2. Maurer-Morelli CV, de Vasconcellos JF, Bruxel EM, Rocha CS, do Canto AM, Tedeschi H, Yasuda CL, Cendes F, Lopes-Cendes I. Gene expression profile suggests different mechanisms underlying sporadic and familial mesial temporal lobe epilepsy. Exp Biol Med (Maywood). 2022 12; 247(24):2233-2250. PMID: 36259630; PMCID: PMC9899983.
      Citations: 2     Fields:    Translation:HumansCells
    3. Bruxel EM, do Canto AM, Bruno DCF, Geraldis JC, Lopes-Cendes I. Multi-omic strategies applied to the study of pharmacoresistance in mesial temporal lobe epilepsy. Epilepsia Open. 2022 08; 7 Suppl 1:S94-S120. PMID: 34486831; PMCID: PMC9340306.
      Citations: 1     Fields:    
    4. Bruxel EM, Bruno DCF, do Canto AM, Geraldis JC, Godoi AB, Martin M, Lopes-Cendes I. Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: Clues into the underlying mechanisms leading to disease. Seizure. 2021 Aug; 90:34-50. PMID: 33722437.
      Citations: 1     Fields:    Translation:Humans
    5. Bruxel EM, Akutagava-Martins GC, Quinn TP, Klein M, Franke B, Kappel DB, Mota NR, Bau CHD, Hutz MH, Moreira-Maia CR, Ribas?s M, Rovira P, S?nchez-Mora C, Grevet EH, Arcos-Burgos M, Rohde LA. Meta-analysis and systematic review of ADGRL3 (LPHN3) polymorphisms in ADHD susceptibility. Mol Psychiatry. 2021 06; 26(6):2277-2285. PMID: 32051549.
      Citations: 7     Fields:    Translation:Humans
    6. Botton MR, Viola PP, Meireles MR, Bruxel EM, Zuchinali P, Bandinelli E, Rohde LE, Leiria TLL, Salamoni JYY, Garbin AP, Hutz MH. Identification of environmental and genetic factors that influence warfarin time in therapeutic range. Genet Mol Biol. 2020; 43(1 suppl 2):e20190025. PMID: 32052826; PMCID: PMC7198020.
      Citations: 2     
    7. Bruxel EM, Akutagava-Martins GC, Genro JP, Zeni CP, Chazan R, Schmitz M, Rohde LA, Hutz MH, Salatino-Oliveira A, Polanczyk GV. GAD1 gene polymorphisms are associated with hyperactivity in Attention-Deficit/Hyperactivity Disorder. Am J Med Genet B Neuropsychiatr Genet. 2016 12; 171(8):1099-1104. PMID: 27530595.
      Citations: 4     Fields:    Translation:Humans
    8. Tovo-Rodrigues L, Recamonde-Mendoza M, Bruxel EM, Schuch JB, Friedrich DC, Rohde LA, Hutz MH, Paix?o-C?rtes VR. The role of protein intrinsic disorder in major psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet. 2016 09; 171(6):848-60. PMID: 27184105.
      Citations: 6     Fields:    Translation:Humans
    9. Akutagava-Martins GC, Bruxel EM, Genro JP, Hutz MH, Salatino-Oliveira A, Polanczyk GV, Zeni C, Kieling C, Karam RG, Rovaris DL, Contini V, Cupertino RB, Mota NR, Grevet EH, Bau CH, Rohde LA. NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children. J Psychiatr Res. 2016 Apr; 75:75-81. PMID: 26821215.
      Citations: 3     Fields:    Translation:Humans
    10. Akutagava-Martins GC, Bruxel EM, Hutz MH, Salatino-Oliveira A, Wagner F, Genro JP, Zeni C, Kieling C, Polanczyk GV, Rohde LA. MAP1B and NOS1 genes are associated with working memory in youths with attention-deficit/hyperactivity disorder. Eur Arch Psychiatry Clin Neurosci. 2016 Jun; 266(4):359-66. PMID: 26233433.
      Citations: 4     Fields:    Translation:Humans
    11. Bruxel EM, Salatino-Oliveira A, Akutagava-Martins GC, Tovo-Rodrigues L, Genro JP, Zeni CP, Polanczyk GV, Chazan R, Schmitz M, Arcos-Burgos M, Rohde LA, Hutz MH. LPHN3 and attention-deficit/hyperactivity disorder: a susceptibility and pharmacogenetic study. Genes Brain Behav. 2015 Jun; 14(5):419-27. PMID: 25989180.
      Citations: 30     Fields:    Translation:HumansCells
    12. Salatino-Oliveira A, Bruxel EM, Genro JP, Mota NR, Polanczyk GV, Zeni CP, Bau CH, Rohde LA, Hutz MH, Akutagava-Martins GC, Grevet EH. Lack of association between the GRM7 gene and attention deficit hyperactivity disorder. Psychiatr Genet. 2014 Dec; 24(6):281-2. PMID: 25360607.
      Citations: 3     Fields:    Translation:Humans
    13. Bruxel EM, Akutagava-Martins GC, Salatino-Oliveira A, Kieling C, Hutz MH, Rohde LA, Contini V. ADHD pharmacogenetics across the life cycle: New findings and perspectives. Am J Med Genet B Neuropsychiatr Genet. 2014 Jun; 165B(4):263-82. PMID: 24804845.
      Citations: 16     Fields:    Translation:Humans
    14. Lima LO, Bruxel EM, Hutz MH, Van der Sand LC, Ferreira ME, Pires RC, Fiegenbaum M, Almeida S, Van der Sand CR. Influence of PPARA, RXRA, NR1I2 and NR1I3 gene polymorphisms on the lipid-lowering efficacy and safety of statin therapy. Arq Bras Endocrinol Metabol. 2013 Oct; 57(7):513-9. PMID: 24232815.
      Citations: 6     Fields:    Translation:Humans
    15. Bruxel EM, Salatino-Oliveira A, Genro JP, Zeni CP, Polanczyk GV, Chazan R, Rohde LA, Hutz MH. Association of a carboxylesterase 1 polymorphism with appetite reduction in children and adolescents with attention-deficit/hyperactivity disorder treated with methylphenidate. Pharmacogenomics J. 2013 Oct; 13(5):476-80. PMID: 22688218.
      Citations: 17     Fields:    Translation:Humans
    16. Sortica VA, Vargens DD, Bruxel EM, Petzl-Erler ML, Petz-Erler ML, Tsuneto LT, Hutz MH, Suarez-Kurtz G. Impact of population diversity on the prediction of 7-SNP NAT2 phenotypes using the tagSNP rs1495741 or paired SNPs. Pharmacogenet Genomics. 2012 Apr; 22(4):305-9. PMID: 22336957.
      Citations: 4     Fields:    Translation:HumansCells
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